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Molecular recognition: Comparative study of a tunable host-guest system by using a fluorescent model system and collision-induced dissociation mass spectrometry on dendrimers

机译:分子识别:通过使用荧光模型系统和碰撞诱导解离质谱法对树枝状聚合物进行可调主客体系统的比较研究

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摘要

Host-guest interactions between the periphery of adamantylurea-functionalized dendrimers (host) and ureido acetic acid derivatives (guest) were shown to be specific, strong and spatially well-defined. The binding becomes stronger when using phosphonic or sulfonic acid derivatives. In the present work we have quantified the binding constants for the host-guest interactions between two different host motifs and six different guest molecules. The host molecules, which resemble the periphery of a poly(propylene imine) dendrimer, have been fitted with an anthracene-based fluorescent probe. The two host motifs differ in terms of the length of the spacer between a tertiary amine and two ureido functionalities. The guest molecules all contain an acidic moiety (either a carboxylic acid, a phosphonic acid, or a sulfonic acid) and three of them also contain an ureido moiety capable of forming multiple hydrogen bonds to the hosts. The binding constants for all 12 host-guest complexes have been determined by using fluorescence titrations by monitoring the increase in fluorescence of the host upon protonation by the addition of the guest. The binding constants could be tuned by changing the design of the acidic part of the guest. The formation of hydrogen bonds gives, in all cases, higher association constants, demonstrating that the host is more than a proton sensor. The host with the longer spacer (propyl) shows higher association constants than the host with the shorter spacer (ethyl). The gain in association constants are higher when the urea function is added to the guests for the host with the longer spacer, indicating a better fit. Collision-induced dissociation mass spectrometry (CID-MS) is used to study the stability of the six motifs using the corresponding third generation dendrimer. A similar trend is found when the six different guests are compared.
机译:金刚烷基脲官能化的树枝状大分子(宿主)和脲基乙酸衍生物(客体)之间的宿主-客体相互作用被证明是特异性的,强的并且在空间上是明确的。当使用膦酸或磺酸衍生物时,结合变得更牢固。在目前的工作中,我们已经量化了两个不同宿主基序和六个不同来宾分子之间宿主-客体相互作用的结合常数。类似于聚亚丙基亚胺树枝状大分子外围的主体分子已安装了基于蒽的荧光探针。这两个主体基序的区别在于叔胺和两个脲基官能团之间的间隔基长度。客体分子均包含酸性部分(羧酸,膦酸或磺酸),其中三个还包含能够与主体形成多个氢键的脲基部分。通过使用荧光滴定法,通过监测添加客体质子化后宿主荧光的增加,已经确定了所有12种宿主-客体复合物的结合常数。可以通过改变客体的酸性部分的设计来调节结合常数。在所有情况下,氢键的形成都赋予较高的缔合常数,表明主体不仅仅是质子传感器。具有较长间隔基(丙基)的主体比具有较短间隔基(乙基)的主体具有更高的缔合常数。当将尿素官能团添加到具有更长间隔基团的主体的客体中时,缔合常数的增益会更高,这表明更好的契合度。碰撞诱导解离质谱(CID-MS)用于使用相应的第三代树状聚合物研究六个基序的稳定性。比较六个不同的客人时,发现了类似的趋势。

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